Instagram
youtube
Facebook

Quality Control Technician Iii

5-10 years
Not Disclosed
10 March 26, 2025
Job Description
Job Type: Full Time Education: M.Sc Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Quality Control Technician III
Date: March 17, 2025
Location: Chennai, India, 600113
Company: Teva Pharmaceuticals
Job ID: 61083


Who We Are:
Teva Pharmaceuticals is a global leader in generic medicines and a key contributor to the World Health Organization’s Essential Medicines List. Operating across nearly 60 countries with a diverse workforce, we strive to make healthcare affordable and accessible, helping millions worldwide enjoy healthier lives. With 200 million people using our medicines daily, we are constantly seeking innovative ways to expand our impact and welcome new talent to contribute to this mission.


How You’ll Spend Your Day:

  • Stability Analysis: Perform stability analysis of pharmaceutical products.

  • Method Transfer/Validation: Conduct method transfer and method validation analysis.

  • Calibration & Validation: Calibrate and validate instruments/equipment used for analysis.

  • Document Preparation: Prepare Method Transfer Protocols (MTP), Method Transfer Reports (MTR), Methods of Analysis (MTH), Test Data Sheets (TDS), and other documents related to stability analysis, method transfer, and validation.

  • Compliance with Guidelines: Ensure all documentation complies with current regulatory guidelines.

  • SOP Development: Prepare departmental Standard Operating Procedures (SOPs) in compliance with current guidelines.

  • Validation Protocols: Prepare validation protocols aligned with regulatory standards.

  • Data Management: Enter stability sample results into LIMS/SAP systems.

  • Software Handling: Manage and operate LSCMS software effectively.


Your Experience and Qualifications:

  • Education: M.Sc. (Chemistry)

  • Experience: 5 to 10 years of relevant experience in stability analysis, method transfer, and method validation.


Teva’s Equal Employment Opportunity Commitment:
Teva Pharmaceuticals is committed to equal opportunity in employment. We ensure that all qualified applicants are considered without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin, or any other legally protected status.

If you are contacted for a job opportunity, please inform us of any accommodations needed to facilitate an inclusive and accessible candidate experience.